Mid-infrared sensor

ABSTRACT

A sensor for monitoring a species which is a component of a fluid. The sensor includes an internal reflection window which, in use, is in direct contact with the fluid. The sensor further includes a mid-infrared light source which directs a beam of mid-infrared radiation into said window for attenuated internal reflection at an interface between the window and the fluid. The sensor further includes a first narrow bandpass filter which preferentially transmits mid-infrared radiation over a band of wavelengths corresponding to an absorbance peak of the species. The sensor further includes an infrared detector which detects filtered mid-infrared radiation transmitted through the first filter and a processor for measuring the intensity of the detected mid-infrared radiation transmitted through the first filter, and determines therefrom an amount of the species in the fluid.

CROSS REFERENCE TO RELATED APPLICATION(S)

This application claims priority as a continuation application of U.S. patent application Ser. No. 15/511,333, filed Mar. 15, 2017, with the same title. The patent application is incorporated by reference in its entirety.

BACKGROUND

Embodiments of the present disclosure relate to a mid-infrared sensor for monitoring a species, which is a component of a fluid.

The analysis of chemical composition of fluid samples from hydrocarbon wells for the determination of phase behaviour and chemical composition is a critical step in the monitoring and management of a hydrocarbon well as well as the evaluation of the producibility and economic value of the hydrocarbon reserves. Similarly, the monitoring of fluid composition during production or other operations can have an important bearing on reservoir management decisions. Similarly, determination of phase behaviour and chemical composition is important in pipelines and the like used to convey/transport hydrocarbons from the wellhead, including subsea pipelines.

Several disclosures have described analysis of specific gases in borehole fluids in the downhole environment using near-infrared (e.g. λ=1-2.5 μm) spectral measurements. For example, U.S. Pat. No. 5,859,430 describes the use of near-infrared spectroscopy to determine quantitatively the presence of methane, ethane and other simple hydrocarbons in the gas phase. The gases were detected using the absorption of near-infrared radiation by the overtone/combination vibrational modes of the molecules in the spectral region 1.64-1.75 μm.

More recently, U.S. Pat. No. 6,995,360 describes the use of mid-infrared radiation with a wavelength λ=3-5 μm to monitor gases in downhole environments, and U.S. Patent. Publication No. 2012/0290208 proposes the use of mid-infrared radiation to monitor sequestered carbon dioxide dissolved into the liquid solutions of saline aquifers.

There are however many technical problems with using mid-infrared sensors in the hydrocarbon industry and processing information from such sensors. Additionally, much of the utility of mid-infrared spectroscopy has not previously been recognized.

SUMMARY

Embodiments of the present disclosure are at least partly based on the recognition that species may be monitored/detected using a sensor based on mid-infrared radiation absorbance. In some embodiments, accuracy of such mid-infrared monitoring ism provided where monitoring temperatures may vary and/or may comprise high or low extremes. In other embodiments, mid-infrared spectroscopy may be used to monitor and/or detect species such as acids, hydrate inhibitors and/or the like.

Accordingly, in a first aspect, an embodiment of the present disclosure provides a sensor for monitoring a species which is a component of a fluid. In the embodiment, the sensor includes an internal reflection window for contacting with the fluid, a mid-infrared light source that directs a beam of mid-infrared radiation into said window sop that the directed beam undergoes attenuated internal reflection at an interface between the window and the fluid, a temperature invariant narrow bandpass filter that preferentially transmits mid-infrared radiation over a band of wavelengths corresponding to an absorbance peak of the species to filter internally reflected mid-infrared radiation received from the window, an infrared detector for detecting filtered mid-infrared radiation transmitted through the filter; and a processor for determining the intensity of the detected mid-infrared radiation transmitted through the first filter. The detected/measured mid-infrared radiation may be used to determine an amount/concentration of the species in the fluid. The temperature invariant narrow bandpass filter is configured such that its wavelength transmission band is substantially temperature invariant over all temperatures in the range from 25 to 150° C.

Temperatures in downhole environments can vary greatly, e.g. from room temperature up to 150° C. or 200° C. In embodiments of the present disclosure, by using a temperature invariant filter, it is possible to use a mid-infrared sensor in a downhole environment and obtain accurate/meaningful measurements.

As discussed below, in embodiments of the present disclosure, the sensor may be part of a sensor arrangement, e.g. with a further similar sensor for obtaining a reference intensity.

In a second aspect, an embodiment of the present disclosure provides the use of the sensor, or sensor arrangement, of the first aspect to determine an amount of a species which is a component of a fluid. For example, a method of monitoring a species which is a component of a fluid may include: providing the sensor of the first aspect such that the internal reflection window is in direct contact with the fluid; and operating the sensor to determine an amount of the species in the fluid.

In a third aspect, an embodiment of the present disclosure provides a well tool (such as a drilling, production well or wireline sampling tool) including the sensor, or sensor arrangement, of the first aspect.

In a fourth aspect, an embodiment of the present disclosure provides a mid-infrared sensor and a method of using such a sensor for detecting/monitoring particular species, including hydrate inhibitors—such as methanol, ethanol, monoethylene glycol, diethylene glycol, polyvinylpyrrolidone, polyvinylcaprolactam and/or the like—and mineral acids.

In a fifth aspect, in accordance with an embodiment of the present disclosure, a method for monitoring a species that is a component of a fluid is provided comprising:

-   -   contacting the fluid with an internal reflection window;     -   directing a beam of mid-infrared radiation into said window to         provide for attenuated internal reflection at an interface         between the window and the fluid;     -   passing the internally reflected mid-infrared radiation from the         window through a first narrow bandpass filter to preferentially         transmit mid-infrared radiation over a band of wavelengths         corresponding to an absorbance peak of the species to filter,         wherein the first narrow bandpass filter is configured to         provide that a wavelength transmission band of the first narrow         bandpass filter is substantially temperature invariant over all         temperatures in the range from about 25 to 150° C.;     -   detecting the filtered mid-infrared radiation transmitted         through the first narrow bandpass filter; and processing an         intensity of the detected mid-infrared radiation transmitted         through the first narrow bandpass filter and an amount of the         species in the fluid.

Optional features of embodiments of the present disclosure will now be set out. These are applicable singly or in any combination with any aspect of the embodiments of the present disclosure.

The fluid may be a liquid, such as a production fluid, drilling fluid, completion fluid or a servicing fluid. The fluid may be a gas, such as a production gas. The fluid may be a liquid/gas mixture.

By “mid-infrared radiation,” it is meant herein that the radiation has a wavelength in the range from about 2 to 20 μm, and in some embodiments from about 3 to 12 μm or from about 3 to 10 μm.

To cover a greater range of downhole temperatures, the wavelength transmission band of the first narrow bandpass filter may be substantially temperature invariant over all temperatures in the range from about 25 to 200° C. To cover both downhole and subsea conditions (where ambient temperatures can be in the range from −25 to 25° C.), the wavelength transmission band of the first narrow bandpass filter may be substantially temperature invariant over all temperatures in the range from about −25 to 125, 150 or 200° C.

By “substantially temperature invariant,” it is meant herein that the variance is at most about 0.1 nm/° C. In some embodiments, the variance is at most about 0.05, 0.03, 0.02 or 0.01 nm/° C.

In some embodiments of the present disclosure, the filter may be an interference filter. For example, the filter may in some embodiments comprise a substrate, formed of Si, SiO₂, Al₂O₃, Ge, ZnSe and/or the like and at each opposing side of the substrate alternating high and low refractive index layers may be formed. For example, in some embodiments, the high refractive index layers may be formed of PbTe, PbSe, PbS and/or the like and the low refractive index layers may be formed of ZnS, ZnSe and/or the like.

In some embodiments of the present disclosure, the filter may comprise three or more half wavelength cavities. Many conventional filters display high band shifts with increasing temperature. For example, shifts in the range 0.2 to 0.6 nm/° C. are typical. Transmissivities of conventional filters also tend to reduce with increasing temperature. However, in embodiments of the present disclosure, by using a PbTe-based, PbSe-based, PbS-based and/or the like interference filter, it is possible to substantially reduce band shifts and transmissivity reductions. For example, a PbTe-based interference filter can, in accordance with an embodiment of the present disclosure, have a band shift of only about 0.03 nm/° C. or less. As an alternative to PbTe, PbSe or PbS, in some embodiments, the high refractive index layers may be formed of Ge or the like.

In some embodiments of the present disclosure, a reference intensity is also used in the determination of the amount of the species in the fluid. Thus a sensor arrangement may include the sensor of the first aspect and a further similar sensor which may be used to obtain this reference intensity. The further sensor can have the same features as the first sensor except that its narrow bandpass filter transmits mid-infrared radiation over a band of wavelengths corresponding to a reference portion of the absorbance spectrum of the fluid. In such a scenario, the processor arrangement can be a shared processor arrangement of both sensors.

Another option, however, is to obtain the reference intensity using the first sensor. For example, the sensor may further include a second narrow bandpass filter transmitting mid-infrared radiation over a band of wavelengths corresponding to a reference portion of the absorbance spectrum of the fluid, the or a further infrared detector detecting filtered mid-infrared radiation transmitted through the second filter, and the processor arrangement measuring the reference intensity of the detected mid-infrared radiation transmitted through the second filter and using the measured reference intensity in the determination of the amount of the species in the fluid. In some embodiments of the present disclosure, the first and second filters may be selectably positionable between a single detector and the window, or each of the first and second filters can have a respective detector. The second narrow bandpass filter may be configured such that its wavelength transmission band is substantially temperature invariant over all temperatures in the range from about 25 to 150° C. Optional features of the first narrow bandpass filter may pertain also to the second narrow bandpass filter.

In some embodiments of the present disclosure, the sensor may be able to measure the amounts of more than one species in the fluid. For example, the sensor may include a plurality of the first narrow bandpass filters, each transmitting mid-infrared radiation over a band of wavelengths corresponding to an absorbance peak of a respective species, the or a respective further infrared detector detecting the filtered mid-infrared radiation transmitted through each first filter, and the processor arrangement measuring the intensity of the detected mid-infrared radiation transmitted through each first filter and determining therefrom an amount of each species in the fluid. In some embodiments of the present disclosure, the first filters may be selectably positionable between a single detector and the window, or each first filter can have a respective detector.

In some embodiments of the present disclosure, when the sensor is able to measure/monitor more than one species, the determined amounts of the species in the fluid may be in the form of a ratio of the concentrations of the species.

In some embodiments of the present disclosure, the beam of mid-infrared light/radiation may be pulsed. This may be achieved, for example, by providing a mechanical chopper between the source and the window, or by pulsing the source.

In some embodiments of the present disclosure, the source may be a broad band thermal source or a narrower band source such as a light emitting diode or a laser.

In some embodiments of the present disclosure, the detector may be a thermopile, a pyroelectric or (particularly in subsea applications, where the low ambient temperatures can provide cooling) a photodiode detector.

In some embodiments of the present disclosure, the window may be a diamond window or a sapphire window. In some embodiments of the present disclosure, the diamond window may be formed by chemical vapour deposition. Sapphire has a cut off for mid-infrared radiation at wavelengths of about 5 to 6 microns, but sapphire windows can generally be formed more cheaply than diamond windows. Thus, for absorption peaks below the cut-off (such as the CO₂ absorption peak at about 4.3 microns), sapphire may be an alternative to diamond. In particular, for a given cost a larger window can be formed.

In some embodiments of the present disclosure, the sensor may further include a heater, which is operable to locally heat the window, thereby cleaning the surface of the window in contact with the fluid. Merely by way of example, in some embodiments of the present disclosure, the window may comprise a conductive or semiconductive material (e.g. an area of semiconductive boron-doped diamond or the like), and the heater may comprise an electrical power supply that sends a current through the window to induce resistive heating thereof. For example, in some embodiments of the present disclosure, the diamond window may comprise a central mid-infrared transmissive (e.g. undoped) area and an encircling area of semiconductive boron-doped diamond. The heater can induce resistive heating of the encircling area, and the central area can then be heated by conduction of heat from the encircling area. In some embodiments of the present disclosure, the heater may heat the window to a peak temperature of at least 400° C. In some embodiments of the present disclosure, the heater may maintain the peak temperature for less than one microsecond.

Alternatively or additionally, in some embodiments of the present disclosure, the sensor may further include an ultrasonic cleaner which is operable to ultrasonically clean the surface of the window in contact with the fluid. As another option, in some embodiments of the present disclosure, the sensor may be provided with a pressure pulse arrangement, which is operable to produce a pressure pulse in the fluid at the window, thereby cleaning the surface of the window in contact with the fluid. In some embodiments of the present disclosure, the arrangement may produce a pressure pulse of at least 1000 psi (6.9 MPa) in the fluid.

In some embodiments of the present disclosure, the sensor may be located downhole.

In some embodiments of the present disclosure, the sensor may be adapted/used for monitoring a hydrocarbon species (typically a constituent chemical group), which is a component of a hydrocarbon liquid. For example, the sensor may be used to determine amounts (e.g. concentrations) of CH₂ and/or CH₃ groups in the liquid. Additionally or alternatively, in some embodiments of the present disclosure, the sensor may determine a ratio of CH₂/CH₃ in the liquid. This ratio and a CH₂ or CH₃ group concentration can be used, for example, to detect whether a drilling fluid based on an unbranched synthetic oil has been contaminated by crude oil.

In some embodiments of the present disclosure, the sensor may be adapted/used for monitoring a hydrate inhibitor species that is dissolved in a liquid. For example, the inhibitor may be a thermodynamic inhibitor such as methanol, ethanol, monoethylene glycol or diethylene glycol, or it may be a kinetic inhibitor such as polyvinylpyrrolidone or polyvinylcaprolactam. In development of an embodiment of the present invention, it was found that mid-infrared spectroscopy could be used to detect/monitor such inhibitors and, advantageously, the positions and heights of the mid-infrared absorbance peak(s) of such compounds tend to be insensitive to salt content in the (typically water-based) liquid. Thus, in embodiments of the present disclosure, the sensitivity of the determination of the amount of the inhibitor to salt concentration can be reduced. For monitoring a hydrate inhibitor, the sensor may, in some embodiments, be adapted for or used in subsea locations, such as subsea pipelines.

In some embodiments of the present disclosure, the sensor may be adapted/used for monitoring a mineral acid species dissolved in a liquid. For example, the mineral acid may be HF, HCl, HBr or HI. HCl in particular is extensively used for stimulation of carbonate formations. In some embodiments of the present disclosure, the sensor provides that the mineral acid concentration may be monitored to evaluate efficiency of acidisation operations; where the high concentrations of mineral acids typically used in such operations often make pH measurements unsuitable. In some embodiments of the present disclosure, the transmission band of the first filter may be located on a dissociated H absorbance peak of about 1050 cm⁻¹. In an embodiment of the present disclosure, the position and height of this peak tends to be insensitive to salt content in the (typically water-based) liquid.

In some embodiments of the present disclosure, the sensor may be adapted/used for monitoring CO₂ concentration in the fluid. In general, attenuated total reflection mid-infrared sensing can only be used to sense condensed phases, but CO₂ is an exception, as it is strongly absorbing in the mid-infrared at a wavelength of about 4.3 μm. In some embodiments of the present disclosure, the sensor may have three first narrow bandpass filters corresponding to respective absorbance peaks of water, oil and CO₂. Such an arrangement can allow the CO₂ concentration to be determined when the window is in contact with a liquid water-based phase, a liquid oil-based phase, a mixture of liquid water and liquid oil-based phases, or a gas phase (i.e. when the window is dry). In some embodiments of the present disclosure, the sensor may also have the second narrow bandpass filter corresponding to a reference portion of the absorbance spectrum of the fluid. The transmission band of the first filters may be located at about 3330 cm⁻¹ (water), 2900 cm⁻¹ (oil) and 2340 cm⁻¹ (CO₂). The transmission band of the second filter may conveniently be located at about 2500 cm⁻¹.

From the above examples, it can be seen that, in some embodiments of the present disclosure, the monitored species may be:

-   -   a compound forming the fluid, or one or more compounds in a         mixture of compounds forming the fluid,     -   a constituent group (e.g. CH₂ or CH₃) of a compound forming the         fluid, or a constituent group common to one or more compounds in         a mixture of compounds forming the fluid,     -   one or more compounds or ions dissolved in a liquid, or     -   a constituent group of a compound or ion dissolved in a liquid,         or a constituent group common to one or more compounds or ions         dissolved in a liquid.

BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the invention will now be described by way of example with reference to the accompanying drawings in which:

FIG. 1A shows schematically a mid-infrared sensor, in accordance with an embodiment of the present disclosure;

FIG. 1B shows schematically the sensor of FIG. 1A implemented as a module in a toolstring;

FIG. 2 shows schematically a narrow bandpass filter based on Fabry-Perot interferometry, in accordance with an embodiment of the present disclosure;

FIG. 3 shows variation of dλ_(m)/λ_(m)dT for a suite of filters fabricated with ZnSe as the low refractive index material and PbTe as the high refractive index material, in accordance with an embodiment of the present disclosure;

FIG. 4A shows a plot of transmissivity against wavelength at a range of temperatures from 25 to 200° C. for a PbTe-based filter having a pass band centred at 4.26 μm, in accordance with embodiments of the present disclosure, and (b)

FIG. 4B shows a plot of transmissivity against wavelength at a range of temperatures from 25 to 200° C. for a PbTe-based filter having a pass band centred at 12.1 μm, in accordance with embodiments of the present disclosure;

FIG. 5A shows a reference intensity spectrum I₀ obtained from a fluid not containing a given species;

FIG. 5B shows an intensity spectrum I obtained from the fluid containing the species of FIG. 5A;

FIG. 5C shows the absorbance spectrum of the species of FIGS. 5A and 5B;

FIG. 6 shows intensity spectra obtained for dodecane dissolved in deuterated chloroform for increasing concentrations of dodecane, the spectra being superimposed with transmissivity plots for a first filter having a pass band of 3000 to 2800 cm⁻¹, and a second filter having a pass band of 2000 to 1800 cm⁻¹;

FIG. 7 shows a plot of modified absorbance A′ against hydrocarbon content for dodecane dissolved in deuterated chloroform;

FIG. 8 shows a plot of absorbance against dissolved CO₂ concentration in water or hydrocarbon;

FIG. 9 shows absorbance spectra of the n-alkane series C₅ to C₁₇;

FIG. 10 shows plots of concentration of CH₂ groups and concentration of CH₃ groups against carbon chain length for the n-alkane series C₅ to C₁₇;

FIG. 11 shows experimentally determined plots of absorbance against concentration of the respective group for n-alkane 2957 cm⁻¹ CH₃ peak, 2853 cm⁻¹ CH₂ peak and 2922 cm⁻¹ CH₂ peak;

FIG. 12 shows mid-infrared absorbance spectra of a number of crude oils, with C₇ and C₁₀ alkane spectra also shown for reference;

FIG. 13 shows the mid-infrared absorbance spectra of the crude oils of FIG. 12 superimposed with the spectra for three common base oils;

FIG. 14 shows again the mid-infrared absorbance spectra of the crude oils of FIG. 12 superimposed with the spectra for two synthetic base oils;

FIG. 15 shows a graph of CH₂/CH₃ ratio against CH₂ group concentration with crude oils plotted as squares and base oils as triangles, and also a curve for n-alkanes;

FIG. 16A shows mid-infrared absorbance spectra of monoethylene glycol in water for different inhibitor concentrations from 0 to 100 vol %;

FIG. 16B shows mid-infrared absorbance spectra of methanol in water for different inhibitor concentrations from 0 to 100 vol %;

FIG. 16C shows mid-infrared absorbance spectra of ethanol in water, for different inhibitor concentrations from 0 to 100 vol %;

FIG. 17A shows a plot of absorbance against inhibitor concentration for-monoethylene glycol in water;

FIG. 17B shows a plot of absorbance against inhibitor concentration for methanol in water;

FIG. 17C shows a plot of absorbance against inhibitor concentration for ethanol in water;

FIG. 18A shows mid-infrared absorbance spectra of 50 vol % monoethylene glycol in water and in water saturated with NaCl;

FIG. 18B shows mid-infrared absorbance spectra of 50 vol % methanol in water and in water saturated with NaCl;

FIG. 18C shows mid-infrared absorbance spectra of 50 vol % ethanol in water and in water saturated with NaCl;

FIG. 19 shows mid-infrared absorbance spectra at 50 vol % water of mixtures of monoethylene glycol and methanol, with the mixtures varying from 100% monoethylene glycol to 100% methanol;

FIG. 20 shows plots of absorbance against concentration for respectively monoethylene glycol (diamonds) based on the leftmost peak of FIG. 19 and methanol (squares) based on the rightmost peak of FIG. 19;

FIG. 21 shows mid-infrared absorbance spectra of polyvinylpyrrolidone in water, for different inhibitor concentrations from 0 to 5 wt %;

FIG. 22 shows a plot of absorbance against inhibitor concentration for polyvinylpyrrolidone in water;

FIG. 23 shows mid-infrared absorbance spectra of 5 wt % polyvinylpyrrolidone in water and in water saturated with NaCl

FIG. 24 shows mid-infrared absorbance spectra of HCl in water, for different HCl concentrations from 0 to 40 wt %;

FIG. 25 shows a plot of absorbance against HCl concentration for HCl in water;

FIG. 26 shows mid-infrared absorbance spectra of DCl in D₂O, for different DCl concentrations from 0 to 35 wt %;

FIG. 27 shows a plot of absorbance against DCl concentration for DCl in D₂O;

FIG. 28 shows mid-infrared absorbance spectra of 4.2 M HCl in water, 4.7 M HBr in water and 4.5 M HI in water;

FIG. 29 shows the plots of absorbance against acid concentration for HCl, HBr and HI in water;

FIG. 30A shows a mid-infrared absorbance spectrum for a water phase and CO₂;

FIG. 30B corresponds to FIG. 30A and shows a plot of absorbance against CO₂ concentration for CO₂ in H₂O;

FIG. 31A shows a mid-infrared absorbance spectrum for an oil phase and CO₂;

FIG. 31B corresponds to FIG. 31A and shows a plot of absorbance against CO₂ concentration for CO₂ in oil;

FIG. 32A shows a mid-infrared absorbance spectrum for a water phase, an oil phase and CO₂; and

FIG. 32B shows a plot of absorbance against CO₂ concentration for CO₂ in gas phase.

In the appended figures, similar components and/or features may have the same reference label. Further, various components of the same type may be distinguished by following the reference label by a dash and a second label that distinguishes among the similar components. If only the first reference label is used in the specification, the description is applicable to any one of the similar components having the same first reference label irrespective of the second reference label.

DETAILED DESCRIPTION

The ensuing description provides preferred exemplary embodiment(s) only, and is not intended to limit the scope, applicability or configuration of the invention. Rather, the ensuing description of the preferred exemplary embodiment(s) will provide those skilled in the art with an enabling description for implementing a preferred exemplary embodiment of the invention, it being understood that various changes may be made in the function and arrangement of elements without departing from the scope of the invention.

Specific details are given in the following description to provide a thorough understanding of the embodiments. However, it will be understood by one of ordinary skill in the art that embodiments maybe practiced without these specific details. For example, well-known circuits, processes, algorithms, structures, and techniques may be shown without unnecessary detail in order to avoid obscuring the embodiments.

Also, it is noted that the embodiments may be described as a process which is depicted as a flowchart, a flow diagram, a data flow diagram, a structure diagram, or a block diagram. Although a flowchart may describe the operations as a sequential process, many of the operations can be performed in parallel or concurrently. In addition, the order of the operations may be re-arranged. A process is terminated when its operations are completed, but could have additional steps not included in the figure. A process may correspond to a method, a function, a procedure, a subroutine, a subprogram, etc. When a process corresponds to a function, its termination corresponds to a return of the function to the calling function or the main function.

Moreover, as disclosed herein, the term “storage medium” may represent one or more devices for storing data, including read only memory (ROM), random access memory (RAM), magnetic RAM, core memory, magnetic disk storage mediums, optical storage mediums, flash memory devices and/or other machine readable mediums for storing information. The term “computer-readable medium” includes, but is not limited to portable or fixed storage devices, optical storage devices, wireless channels and various other mediums capable of storing, containing or carrying instruction(s) and/or data.

Furthermore, embodiments may be implemented by hardware, software, firmware, middleware, microcode, hardware description languages, or any combination thereof. When implemented in software, firmware, middleware or microcode, the program code or code segments to perform the necessary tasks may be stored in a machine readable medium such as storage medium. A processor(s) may perform the necessary tasks. A code segment may represent a procedure, a function, a subprogram, a program, a routine, a subroutine, a module, a software package, a class, or any combination of instructions, data structures, or program statements. A code segment may be coupled to another code segment or a hardware circuit by passing and/or receiving information, data, arguments, parameters, or memory contents. Information, arguments, parameters, data, etc. may be passed, forwarded, or transmitted via any suitable means including memory sharing, message passing, token passing, network transmission, etc.

It is to be understood that the following disclosure provides many different embodiments, or examples, for implementing different features of various embodiments. Specific examples of components and arrangements are described below to simplify the present disclosure. These are, of course, merely examples and are not intended to be limiting. In addition, the present disclosure may repeat reference numerals and/or letters in the various examples. This repetition is for the purpose of simplicity and clarity and does not in itself dictate a relationship between the various embodiments and/or configurations discussed. Moreover, the formation of a first feature over or on a second feature in the description that follows may include embodiments in which the first and second features are formed in direct contact, and may also include embodiments in which additional features may be formed interposing the first and second features, such that the first and second features may not be in direct contact.

FIG. 1A shows schematically a mid-infrared sensor, in accordance with an embodiment of the present disclosure, comprising a thermal broad band mid-infrared source 1, a mechanical chopper 2 that pulses a beam 3 of mid-infrared radiation which issues from the source, a diamond window 4, a set of selectively movable first narrow bandpass filters 5 and a second narrow bandpass filter 5′, respective mid-infrared detectors 6 for the filters, and a processor arrangement 7. The sensor may be encased in a protective housing which allows the sensor to be deployed downhole, the window 4 being positioned for contact with the fluid to be monitored. In some embodiments of the present disclosure, mid-infrared waveguides (not shown) may optically connect the source, window and the detectors. Suitable waveguides can be formed from optical fibres (e.g. hollow fibres or chalcogenide fibres), solid light pipes (e.g. sapphire pipes), or hollow light pipes (e.g. air or vacuum filled) with a reflective (e.g. gold) coating.

As the output from detector 6 changes with temperature, even small changes in temperature may cause a large drift in signal output. However, in some embodiments of the present disclosure, pulsing the beam 3 allows the output signal of the detector to be frequency modulated, enabling removal of the environmental temperature effects from the signal. More particularly, the environment effects can be largely removed electronically by a high pass filter, because the time constant for environment effects tends to be much longer than the signal frequency. In some embodiments of the present disclosure, the detector output is AC-coupled to an amplifier. The desired signal can then be extracted e.g. electronically by lock-in amplification or computationally by Fourier transformation.

Instead of the thermal source 1 and the mechanical chopper 2, in some embodiments of the present disclosure, the pulsed beam 3 may be produced by a pulsable thermal source, light emitting diode or laser source and/or the like. Pulsing the source in this way can give the same benefit of frequency modulation measurement, plus it may reduce resistive heating effects.

The beam 3 enters at one edge of the window 4, and undergoes a number of total internal reflections before emerging from the opposite edge. The total internal reflection of the infrared radiation at the fluid side of the window is accompanied by the propagation of an evanescent wave into the fluid. As the fluid preferentially absorbs certain wavelengths, depending on its chemical composition, this causes the emerging beam to have a characteristic variation in intensity with wavelength.

In some embodiments of the present disclosure, the window 4 may be mechanically able to withstand the high pressures and temperatures typically encountered downhole. In some embodiments of the present disclosure, the window may be chemically stable to fluids encountered downhole and transparent in the mid-IR wavelength region. In some embodiments of the present disclosure, the window may comprise diamond, sapphire and/or the like.

The first narrow bandpass filters 5 each transmit mid-infrared radiation over a band of wavelengths corresponding to an absorbance peak of a respective species in the fluid, while the second narrow bandpass filter 5′ transmits mid-infrared radiation over a band of wavelengths corresponding to a reference portion of the absorbance spectrum of the fluid. The beam 3 then passes through a selected one of the narrow bandpass filters and is detected at the respective detector 6. Instead of having a plurality of detectors, each movable with its corresponding filter (as indicated by the double-headed arrow), a further option is to have a single detector in front of which the filters are selectively movable.

The detector 6 may comprise semiconductor photo-diodes (particularly in subsea applications), thermopiles or pyroelectric detectors.

an embodiment of the present disclosure the processor arrangement 7 receives a signal from the respective detector 6, which it processes to measure the intensity of the detected mid-infrared radiation transmitted through each filter 5, 5′, and may either detect the respective species in the fluid or determine from the measured intensity, as discussed in more detail below, an amount of the respective species in the fluid.

Also discussed in more detail below, the sensor comprise have a heater 8 which is operable to locally heat the window 4, thereby cleaning the surface of the window in contact with the fluid. Other options, however, are to clean the window ultrasonically (as described for example in U.S. Pat. No. 7,804,598 incorporated by reference herein for all purposes), or with a mechanical wiper.

FIG. 1B shows schematically how the sensor, in accordance with embodiments of the present disclosure may be implemented as a module in a toolstring. In an embodiment of the present disclosure, the source 1 and chopper 2 may be contained in a source unit 9 and filters 5, 5′ and detectors 6 may be contained in a detector unit 10. These are located close to the window 4 that is in contact with a tool flowline 11. In some embodiments of the present disclosure, the sensor is packaged in a protective metal chassis 12 to withstand the high pressure of the fluid in the flowline. In some embodiments of the present disclosure, the window is sealed into the chassis also to withstand the high pressures, and its packaging ensures no direct source light strays into the detectors.

Narrow Bandpass Filters

In some embodiments of the present disclosure, the narrow bandpass filters 5, 5′ may be based on Fabry-Perot interferometry. As shown in FIG. 2, in some embodiments of the present disclosure, each filter may comprise a substrate S of low refractive index and thickness d. On opposing surfaces of the substrate are stacked alternating high-reflectivity dielectric layers of high H and low L refractive index deposited onto the substrate using techniques such as ion-beam sputtering or radical-assisted sputtering. Each layer in the stacks of alternating layers of high H and low L refractive index has an optical thickness of a quarter wavelength.

In an embodiment of the present disclosure, the optical thickness nd cos θ of the substrate S, where n is the refractive index of the substrate, is equal to an integer number of half wavelengths λ_(m), where λ_(m) is the peak transmission wavelength, corresponding approximately to the centre wavelength of the pass band of the filter. The condition for the transmission of radiation of wavelength λ_(m) through the filter is thus mλ_(m)/2=nd cos θ, where m is an integer.

The spectral region of conventional narrow bandpass dielectric filters designed to operate in the mid-infrared spectral regions shifts systematically to longer wavelengths with increasing temperature. The origin of the change in λ_(m) with temperature is a change in the material properties with temperature of the dielectric materials that comprise the layers of the filter.

However, in accordance with embodiments of the present disclosure, an approach for the configuration and fabrication of mid-infrared narrow bandpass filters is provided where the filters have substantially temperature invariant optical properties over a wide temperature range.

In accordance with embodiments of the present disclosure, the approach can be considered by the design of the filter: (LH)^(x1)(LL)^(y1)(HL)^(x2)(LL)^(y2) . . . (LL)^(yN)(HL)^(xN+1)

consisting of a total of y half wavelength spacers (cavities) LL of low refractive index material in N cycles (y=Σ_(i), LH being the stacks of x_(i) quarter wavelength layers of alternating of high and low refractive index material in the N cycles. The reflections wavelength of the quarter wavelength reflector stack (which is the only reflection to undergo constructive interference), irrespective of the values of x_(i) and N, can be expressed as: λ_(m)=2(n _(L) d _(L) +n _(H) d _(H))

for first order reflections (m=0). The temperature variation of the wavelength in the reflector stack dλ_(m)/dT|_(s) can be expressed as:

${\frac{d\;\lambda_{m}}{dT}\text{|}_{s}} = {{2n_{L}{d_{L}\left( {C_{L} + \frac{{dn}_{L}}{n_{L}{dT}}} \right)}} + {2n_{H}{d_{H}\left( {C_{H} + \frac{{dn}_{H}}{n_{H}{dT}}} \right)}}}$

where C_(L) and C_(H) are the coefficients of linear expansion of the low and high refractive index materials, respectively. From eqn. [1] for first order reflection and normal incidence (i.e., m=1 and θ=0°), the corresponding temperature dependence dλ_(m)/dT|_(c) of the cavity layer of low refractive index material is given by:

${\frac{d\;\lambda_{m}}{dT}\text{|}_{c}} = {2{yn}_{L}{d_{L}\left( {C_{L} + \frac{{dn}_{L}}{n_{L}{dT}}} \right)}}$

noting that y is the total number of half wavelength cavity layers. The total change in wavelength with temperature dλ_(m)/dT|_(T) is given by the sum of dλ_(m)/dT|_(c) and dλ_(m)/dT|_(s);

${\frac{d\;\lambda_{m}}{dT}\text{|}_{T}} = {{2\left( {1 + y} \right)n_{L}{d_{L}\left( {C_{L} + \frac{{dn}_{L}}{n_{L}{dT}}} \right)}} + {2n_{H}{d_{H}\left( {C_{H} + \frac{{dn}_{H}}{n_{H}{dT}}} \right)}\mspace{14mu}{or}}}$ ${\frac{d\;\lambda_{m}}{\lambda_{m}{dT}}\text{|}_{T}} = {{\left( {1 + y} \right)\left( {C_{L} + \frac{{dn}_{L}}{n_{L}{dT}}} \right)} + \left( {C_{H} + \frac{{dn}_{H}}{n_{H}{dT}}} \right)}$ noting that n_(L)d_(L)=n_(H)d_(H) at the temperature for which the filter is designed for use. Clearly dλ_(m)/dT|_(T) can only be zero if the value of dn/dT for one of the materials is negative. This condition can be fulfilled by high refractive index materials such as PbTe, PbSe or PbS. For close matching of the value of dλ_(m)/dT|_(T) to zero, the wavelength dependence of n_(i) temperature and wavelength dependence of dn_(i)/dT can be taken into account.

The condition dλ_(m)/dT|_(T)=0 is given approximately by:

$\frac{{dn}_{H}}{n_{H}{dT}} = {{- \left( {1 + y} \right)}\frac{{dn}_{L}}{n_{L}{dT}}}$

noting that C_(i) is considerably smaller than dn_(i)/n_(i)dT for most materials used in mid-infrared filters. The term (1+y) can be chosen to satisfy the above expression depending on the choice of low refractive index material. For example, with ZnSe and PbTe for the low and high refractive index materials, respectively, and using the material values of bulk phases n_(L)=2.43, n_(H)=6.10, dn_(L)/dT=6.3×10⁻⁵ K⁻¹ and dn_(H)/dT=−2.1×10⁻³ K⁻¹ for λ_(m)=3.4 μm, the expression is satisfied with y=13.3, i.e., approximately 13 half wavelength cavity layers are required to achieve the condition dλ_(m)/dT|_(T)=0.

There is considerable variation in the values of the material properties (n_(H), dn_(H)/dT, C_(H), etc.) that appear in for thin films in a multilayer structure and therefore in the predicted value of dλ_(m)/dT_(T) or the value of y required to achieve the condition dλ_(m)/λ_(m)dT=0. The uncertainty is particularly severe for the value of dn_(H)/dT for PbTe in view of its magnitude and influence on the value of y. For example, the value of dn/dT for PbTe at λ_(m)=5 μm has been reported to be −1.5×10⁻³ K⁻¹ by Zemel, J. N., Jensen, J. D. and Schoolar, R. B., “ELECTRICAL AND OPTICAL PROPERTIES OF EPITAXIAL FILMS OF PBS, PBSE, PBTE AND SNTE ”, Phys. Rev. 140, A330-A343 (1965), −2.7×10⁻³ K⁻¹ by Piccioli, N., Besson, J. M. and Balkanski, M., “OPTICAL CONSTANTS AND BAND GAP OF PBTE FROM THIN FILM STUDIES BETWEEN 25 AND 300° K.”, J. Phys. Chem. Solids, 35, 971-977 (1974), and −2.8×10⁻³ K⁻¹ by Weiting, F. and Yixun, Y., “TEMPERATURE EFFECTS ON THE REFRACTIVE INDEX OF LEAD TELLURIDE AND ZINC SELENIDE ”, Infrared Phys., 30, 371-373 (1990). From the above expression, the corresponding values of y (to the nearest integer) are 9, 17 and 18, respectively.

In view of the uncertainties in the value of dn/dT for PbTe and therefore the number of low refractive index half wavelength spacers required to achieve dλ_(m)/dT=0, a more useful approach is to determine the experimental value of dλ_(m)/dT as a function of the optical thickness of the low refractive index cavities for a suite of filters fabricated by the same method.

FIG. 3 shows the variation of dλ_(m)/λ_(m)dT for a suite of filters fabricated with ZnSe as the low refractive index material and PbTe as the high refractive index material. The plot shows that a particular value of dλ_(m)/λ_(m)dT can be achieved by controlling the ratio of low to high refractive index materials in the filter (i.e., a parameter similar to y in the above expression). FIG. 3 shows that for λ_(m)<5 μm, the condition dλ_(m)/λ_(m)dT=0 is met by a 4:4:4 (i.e., 3 full wavelength or 6 half wavelength cavities (y=6)) filter, while for λ_(m)>5 μm a 6:4:6 (y=8) filter is required.

The approach illustrated by FIG. 3 can be used, in accordance with an embodiment of the present disclosure, to fabricate substantially temperature invariant filters over the entire mid-infrared spectral range. In some embodiments of the present disclosure, the substrate may be formed of Si, SiO₂, Al₂O₃, Ge or ZnSe. In some embodiments of the present disclosure, high refractive index layers can be formed of PbTe, PbSe or PbS, although Ge is also an option. In some embodiments of the present disclosure, the low refractive index layers can be formed of ZnS or ZnSe.

FIGS. 4A and 4B show plots of transmissivity against wavelength at a range of temperatures from 25 to 200° C. FIG. 4A shows a plot for a PbTe-based filter having a pass band centred at 4.26 μm with optimum optical matching to the substrate and 3 full wavelength thickness cavities (4:4:4), and FIG. 4B shows a plot for a degenerate PbTe-based filter having a pass band centred at 12.1 μm with 3 half wavelength cavities (2:2:2). Similar filters can be produced having pass bands centred at other mid-infrared wavelengths. The value of dλ_(m)/dT for the λ_(m)=4.26 μm (4:4:4) filter varies from −0.04 nm/K at 20° C. to +0.03 nm/K at 200° C. and is essentially zero over the temperature range 80-160° C. The value of dλ_(m)/dT for the λ_(m)=12.1 μm (2:2:2) filter is −0.21 nm/K, over the temperature range 20-200° C. This allows such filters to deployed downhole, where temperatures can vary from about 25 to 200° C., without the pass band of the filter shifting to such an extent that it no longer corresponds to the absorbance peak of its respective species.

Spectroscopy

The Beer-Lambert law applied to the sensor of FIGS. 1A and 1B provides that: A=−log₁₀(I/I ₀)

where A is the absorbance spectrum by a species in the fluid having an absorbance peak at a wavelengths corresponding to the pass band of the filter 5, I is the intensity spectrum of the infrared radiation detected by the detector 6, and I₀ is a reference intensity spectrum. For example, FIGS. 5A to 5C show (a) a reference intensity spectrum I₀ obtained from a fluid not containing a given species, (b) an intensity spectrum I obtained from the fluid containing the species, and (c) the absorbance spectrum of the species.

FIG. 6 shows intensity spectra obtained for dodecane dissolved in deuterated chloroform for increasing concentrations of dodecane. With increasing hydrocarbon content there is increased absorption in a first wavenumber range of 3000 to 2800 cm⁻¹. Conversely, the increasing hydrocarbon content has substantially no effect on absorption in a second wavenumber range of 2000 to 1800 cm⁻¹. The second range can thus be used as the reference to the first range. Superimposed on FIG. 6 are transmissivity plots for a first filter having a pass band of 3000 to 2800 cm⁻¹, and a second filter having a pass band of 2000 to 1800 cm⁻¹. Two spectra are thus, in effect, detected by the filters, the first spectrum being the unfiltered spectrum multiplied by the transmissivity of the first filter and the second sub-spectrum being the unfiltered spectrum multiplied by the transmissivity of the second filter. The pass band areas of the spectra (as determined by the strengths of the signals received by the photodiode detectors), correspond to respective intensity measurements BA and BA₀. These are thus used to calculate a modified absorbance A′ for dodecane dissolved in deuterated chloroform which is ln(BA/BA₀.

FIG. 7 shows a plot of modified absorbance A′ against hydrocarbon content for dodecane dissolved in deuterated chloroform. The plot exhibits an approximately linear relationship between A′ and hydrocarbon content.

Other species can be monitored in this way. For example, FIG. 8 shows a plot of absorbance against dissolved CO₂ concentration in water or hydrocarbon under the high partial pressures and temperatures typical of oil field wellbore conditions.

Hydrocarbon Characterisation

A mid-infrared sensor in accordance with an embodiment of the present disclosure may be used to characterise hydrocarbons downhole. The ability of the sensor to operate under a full range of downhole temperatures, among other things, is particularly advantageous. The sensor may be deployed, for example, in a drilling, production well or wireline sampling tool.

FIG. 9 shows absorbance spectra of the n-alkane series C₅ to C₁₇. The mid-infrared spectrum is largely determined by CH₂ and CH₃ groups. FIG. 10 shows plots of concentration of CH₂ groups and concentration of CH₃ groups against carbon chain length. With increasing chain length, the relative number of CH₂ to CH₃ groups increases. This is reflected in FIG. 9 by the CH₂ peaks increasing in height and the CH₃ peaks decreasing in height as the chain length increases.

FIG. 11 shows experimentally determined plots of absorbance against concentration of the respective group for the 2957 cm⁻¹ CH₃ peak, the 2853 cm⁻¹ CH₂ peak and the 2922 cm⁻¹ CH₂ peak. The plots demonstrate for all peaks reasonable linearity between absorbance and concentration (e.g. A(2957 cm⁻¹)=0.0068[CH₃]+0.030 and e.g. A(2853 cm⁻¹)=0.0065[CH₂]−0.127), and also reasonable sensitivity of absorbance to change in concentration.

Thus one option, in accordance with an embodiment of the present disclosure, is to perform quantitative analysis of CH₂ or CH₃ group concentration based on infrared intensity measurements (a) filtered over a band corresponding to a respective peak of the dissolved species and (b) filtered over a band corresponding to a reference portion of the absorbance spectrum.

Another option, in accordance with an embodiment of the present disclosure, is to use filters having pass bands at, for example, 2957 cm⁻¹ (for CH₃) and 2841 cm⁻¹ (for CH₂) to enable the CH₂/CH₃ ratio to be determined. This can useful for detecting contamination of oil-based drill fluids by crude oil during sampling.

In particular, crude oils show only modest variation in CH₂/CH₃ ratio.

FIG. 12 shows mid-infrared absorbance spectra of a number of crude oils, with C₇ and C₁₀ alkane spectra also shown for reference. For North Sea crude the CH₂/CH₃ ratio is 3.48, for Cold Lake heavy oil is 3.65 and for Marmul crude it is 4.22. The CH₂/CH₃ ratios are thus within the range of n-alkanes C₈-C₁₁. FIG. 13 shows the mid-infrared absorbance spectra of the same crude oils superimposed with the spectra for three common base oils (HT 40N a, Escaid 110 and Clairsol 370). There is little discrimination between the spectra of the crude oils and the base oils. However, use of a synthetic base oil consisting of straight-chain alkanes enhances the contrast in the CH₂/CH₃ ratio. For example, Biobase 300 base oil available from M-I has a CH₂/CH₃ ratio of 4.13 and Sipdrill 2/0 base oil also from M-I has a CH₂/CH₃ ratio of 4.84.

FIG. 14 shows again the mid-infrared absorbance spectra of the crude oils but now superimposed with the spectra for these two synthetic base oils.

Thus, using a reference filter and respective filters for CH₂ and for CH₃, in accordance with an embodiment of the present disclosure, allows an oil to be plotted on a graph of CH₂/CH₃ ratio against CH₂ group concentration.

FIG. 15 shows such a graph, with crude oils plotted as squares and base oils as triangles, and for reference the curve for n-alkanes also provided. Broadening of spectra for crude oils over base oils is one of the reasons why crude oils tend to exhibit higher a CH₂/CH₃ ratio for a given CH₂ group concentration than base oils. Nonetheless, the two triangles at far right are the Biobase 300 and Sipdrill 2/0 synthetic base oils, demonstrating that such a plot provides a basis for discriminating between synthetic non-branched base oils and crude oils and thus detecting base oil contamination by crude oil.

Hydrate Inhibitor Concentration

A further possible use for a sensor in accordance with an embodiment of the present disclosure is to monitor hydrate inhibitor concentrations, for example in subsea locations, such as subsea pipelines.

In the hydro-carbon industry, gas hydrates can form, particularly, in production pipelines. This is undesirable as the hydrates can agglomerate and block the flow and/or cause equipment damage. Two solutions are generally proposed. One is to add thermodynamic inhibitors, such as methanol, ethanol, monoethylene glycol or diethylene glycol, to the flow. These compounds may be recovered and recirculated. Although such thermodynamic inhibitors are cheap, they usually have to be added in large quantities in order to have a thermodynamic effect of lowering the hydrate formation temperature and/or delaying hydrate formation. The second is to add kinetic inhibitors, such as polyvinylpyrrolidone or polyvinylcaprolactam, to the flow. These work by slowing down the rate of hydrate nucleation and/or reducing hydrate agglomeration. They can be effective in lower doses, but are more expensive than most thermodynamic inhibitors.

With both types of inhibitor it is important to be able to measure the concentration of inhibitor in the liquid. Salt can be present in the liquid, sometimes in varying amounts, and may make such measurements problematic. However, the positions of mid-infrared absorption peaks of many inhibitors are not sensitive to salt concentration, making a mid-infrared sensor in accordance with an embodiment of the present disclosure an attractive proposition for measuring inhibitor concentration.

FIGS. 16A to 16C show mid-infrared absorbance spectra of (a) monoethylene glycol in water, (b) methanol in water, and (c) ethanol in water, for different inhibitor concentrations from 0 to 100 vol %.

FIGS. 17A to 17C show plots of absorbance against inhibitor concentration for (a) monoethylene glycol in water, (b) methanol in water, and (c) ethanol in water. For FIG. 17A, the absorbances were measured using a band located on the 1084 cm⁻¹ absorbance peak and a band corresponding to a reference portion of the absorbance spectrum. For FIG. 17B, the absorbances were measured using a band located on the 1020 cm⁻¹ absorbance peak and a band corresponding to a reference portion of the absorbance spectrum. For FIG. 17C, the absorbances were measured using a band located on the 1045 cm⁻¹ absorbance peak and a band corresponding to a reference portion of the absorbance spectrum. The plots of FIGS. 17A to 17C demonstrate good linearity between absorbance and concentration.

FIGS. 18A to 18C show mid-infrared absorbance spectra of (a) 50 vol % monoethylene glycol in water and in water saturated with NaCl, (b) 50 vol % methanol in water and in water saturated with NaCl, and (c) 50 vol % ethanol in water and in water saturated with NaCl. For monoethylene glycol, the 1084 cm⁻¹ absorbance peak shifts in the presence of NaCl, but the position of an alternative 1040 cm⁻¹ absorbance peak is static. This illustrates how a mid-infrared sensor in accordance with the present disclosure may be used to measure species, such as monoethylene glycol in the presence of NaCl. In particular, the mid-infrared sensor can be tuned, i.e., the filter can be tuned, to account for absorbance peak shifts in the presence of NaCl. For methanol, the position of the 1020 cm⁻¹ absorbance peak is static, and for ethanol the position of the 1044 cm⁻¹ absorbance peak is static.

FIG. 19 shows mid-infrared absorbance spectra at 50 vol % water of mixtures of monoethylene glycol and methanol, with the mixtures varying from 100% monoethylene glycol to 100% methanol. The right hand peak grows with increasing methanol, and the two left hand peaks grow with increasing monoethylene glycol. FIG. 20 shows plots of absorbance against concentration for respectively monoethylene glycol (diamonds) based on the leftmost peak and methanol (squares) based on the rightmost peak. Relative amounts of monoethylene glycol and methanol in a mixture can be determined from such plots.

FIG. 21 shows mid-infrared absorbance spectra of polyvinylpyrrolidone in water, for different inhibitor concentrations from 0 to 5 wt %, and FIG. 22 shows a plot of absorbance against inhibitor concentration for polyvinylpyrrolidone in water, using a band located on the 1295 cm⁻¹ absorbance peak and a band corresponding to a reference portion of the absorbance spectrum. The plot of FIG. 22 demonstrates good linearity between absorbance and concentration. FIG. 23 shows mid-infrared absorbance spectra of 5 wt % polyvinylpyrrolidone in water and in water saturated with NaCl, the position of the 1295 cm⁻¹ absorbance peak being static. Thus as with the other species, such an inhibitor can be measured in the presence of salt as absorption can be differentiated and/or the sensor can be tuned for movement of the peaks in the presence of salt.

Mineral Acid Concentration

Another possible use for a sensor in accordance with an embodiment of the present disclosure is to monitor mineral acid concentrations. Mineral acid measurement/monitoring is problematic in general because of the nature of the acids and the effect the acids have on sensor systems. However, the inventors have found that, surprisingly, acid concentration may be determined from mid-infrared spectroscopy.

Mineral acids may be in many industries, including the petroleum industry. For example, HCl is extensively pumped downhole for stimulation of carbonate formations. The high mineral acid concentration typically used in such operations often makes pH measurements unsuitable. However, the sensor in accordance with an embodiment of the present disclosure may be deployed to enable HCl concentration to be monitored to evaluate acidisation efficiency. The ability of the sensor in accordance with the first aspect of the present disclosure to operate under a full range of downhole temperatures may also be advantageous.

FIG. 24 shows mid-infrared absorbance spectra of HCl in water, for different HCl concentrations from 0 to 40 wt %, and FIG. 25 shows a plot of absorbance against HCl concentration for HCl in water, using a band located on the 1050 cm⁻¹ absorbance peak and a band corresponding to a reference portion of the absorbance spectrum. The plot of FIG. 25 demonstrates good linearity between absorbance and concentration. NaCl is not a factor with respect to HCl use in the petrochemical industry, however, CaCl will be a return product in downhole HCl applications.

The 1050 cm⁻¹ absorbance peak is apparently due to dissociated HCl, the peak only emerging as the HCl concentration rises. Further evidence that the peak is due to dissociated HCl comes from measurements of DCl in D₂O. FIG. 26 shows mid-infrared absorbance spectra of DCl in D₂O, for different DCl concentrations from 0 to 35 wt %. As expected, all the peaks shown in FIG. 24 are shifted in FIG. 26 to lower wavenumbers by approximately 1/√2. For completeness, FIG. 27 shows a plot of absorbance against DCl concentration for DCl in D₂O, using a band located on the 850 cm⁻¹ absorbance peak (shifted from 1050 cm⁻¹ in FIG. 24) and a band corresponding to a reference portion of the absorbance spectrum.

The 1050 cm⁻¹ absorbance peak is also exhibited by HBr and HI, as illustrated by FIG. 28 which shows mid-infrared absorbance spectra of 4.2 M HCl in water, 4.7 M HBr in water and 4.5 M HI in water, suggesting that the peak is caused by a hydrated proton. FIG. 29 shows the corresponding plots of absorbance against acid concentration using a band located on the 1050 cm⁻¹ absorbance peak.

Carbon Dioxide Concentration

Another possible use for a sensor in accordance with an embodiment of the present disclosure is to monitor CO₂ concentrations. The analysis of fluid samples from hydrocarbon wells for the determination of phase behaviour and chemical composition is a critical step in the evaluation of the producibility and economic value of the hydrocarbon reserves. An important factor in determining the economic value of gas and liquid hydrocarbon reserves is their chemical composition, particularly the concentration of gaseous components, such as carbon dioxide. Similarly, the monitoring of fluid composition during production operations can have an important bearing on reservoir management decisions, such as ceasing production from certain zones or applying chemical treatments to producing wells.

A mid-infrared sensor, in accordance with an embodiment of the present disclosure comprising a temperature invariant filter, may be used to monitor CO₂ concentrations downhole. In particular, in accordance with embodiments of the present disclosure, the sensor may comprise three narrow bandpass filters 5 corresponding to respective absorbance peaks of water, oil and CO₂, and a second narrow bandpass filter 5′ for a reference portion of the absorbance spectrum. Such an arrangement allows the CO₂ concentration to be determined when the window 4 is wetted by a liquid water phase, a liquid oil phase, a mixture of liquid water and liquid oil phases, or when the window is dry.

For example, FIG. 30A shows an absorbance spectrum for the case where the window 4 is wetted by a water phase. The spectrum is characterised by high absorption by water at 3.00 μm, almost no absorption by oil at 3.45 μm. The CO₂ concentration is proportional to the net CO₂ absorption, which is the difference between the CO₂ channel at 4.27 μm and the reference channel at 4.00 μm. The proportionality constant allowing CO₂ concentration in the water phase to be determined from CO₂ absorption can be obtained from an experimental plot of CO₂ absorbance against dissolved CO₂ concentration in water, such as shown in FIG. 30B.

Similarly, FIG. 31A shows an absorbance spectrum for the case where the window 4 is wetted by an oil phase. The spectrum is characterised by high absorption by oil at 3.45 um μm almost no absorption by water at 3.00 μm. Again, the CO₂ concentration is proportional to the net CO₂ absorption, which is the difference between the CO₂ channel at 4.27 μm and the reference channel at 4.00 μm. The proportionality constant allowing CO₂ concentration in the oil phase to be determined from CO₂ absorption can be obtained from an experimental plot of CO₂ absorbance against dissolved CO₂ concentration in oil, such as shown in FIG. 31B.

Next, FIG. 32A shows an absorbance spectrum for the case where the window 4 is wetted by a mixture of water and oil phases. The spectrum is characterised by absorption by water at 3.00 μm and by oil at 3.45 μm. Again the CO₂ concentration is proportional to the net CO₂ absorption, which is the difference between the CO₂ channel at 4.27 μm and the reference channel at 4.00 μm. However, the proportionality constant is slightly different for water and for oil because their refractive indices, and thus their depths of investigation, are different.

Specifically, oil has higher refractive index than water, thus its depth of investigation is deeper and potentially more CO₂ is sensed by the sensor in oil than in water. Thus, when the window is wetted by a mixture of both water and oil phase, the mixture proportionality constant is between those of water and oil, but can be calculated. For example, a simple approach is to use a “lever rule”, whereby if the water peak height is X % of its full height and the oil peak height is (100−X) % of its full height, the mixture proportionality constant is the sum of X % of the water proportionality constant and (100−X) % of the oil proportionality constant. More elaborate schemes can be used, but the simple “lever rule” approach works reasonably well because the difference between the water and oil proportionality constants is in any event not great.

Under some circumstances, the sensor window 5 may be dry. The spectrum is characterised by almost no absorption by water at 3.00 μm or by oil at 3.45 μm. CO₂ concentration is proportional to the net CO₂ absorption, which is the difference between the CO₂ channel at 4.27 μm and the reference channel at 4.00 μm. The proportionality constant allowing CO₂ concentration in the gas phase to be determined from CO₂ absorption can be obtained from an experimental plot of CO₂ absorbance against CO₂ concentration in gas phase, such as shown in FIG. 32B.

Monitoring of CO₂ concentration can be particularly useful when performed in combination with monitoring of mineral acid concentrations. In particular, the mineral acid sensor can provide a measure of how much acid is being deployed to stimulate a carbonate formation, and the CO₂ sensor, by measuring the amount of CO₂ produced, can provide a measure of the effectiveness of that acid deployment. As such, in some embodiments of the present disclosure, a combination sensor may be used to measure the CO₂ and mineral acid concentrations.

Heater

As mentioned above, the sensor of FIGS. 1A and 1B may comprise a heater 8 which is operable to locally heat the window 4, thereby cleaning the surface of the window in contact with the fluid.

Cleaning the window in this manner is particularly effective, compared to other techniques such as ultrasonic cleaning or mechanical wiper cleaning.

The window 4 can be formed, for example, of diamond (e.g. by chemical vapour deposition). In some embodiments of the present disclosure, a central (typically undoped) area of the window can be mid-infrared transmissive, while an annular encircling area of the window can be made semiconductive, e.g. by boron doping that part of the window. The heater 8 may comprise a simple electrical power source which sends a current through the window to induce resistive heating of the encircling area. The central area of the window is then heated by thermal conduction from the encircling area. Boron-doping of diamond components is discussed in U.S. Pat. No. 7,407,566, which is incorporated by reference herein for all purposes.

In some embodiments of the present disclosure, the heater 8 may be able to heat the window to at least about 400° C. This is higher than the 374° C. super-critical point for water, where super-critical water is a good cleaner and oxidiser. In embodiments of the present disclosure, it may be unnecessary to keep the window at high temperature for a long time period. In particular, less than a microsecond at peak temperature may be enough for cleaning purposes, with longer periods requiring more power and increasing the risk of overheating of other parts of the sensor.

Pressure Pulse Cleaner

In addition, or as an alternative, to the above heater, cleaning of the window 4 may, in some embodiments of the present disclosure, be performed by providing the sensor with a pressure pulse arrangement. For example, the sensor may be located on a fluid flow line between a pump for the fluid and an exit port from the flow line. With the exit port in a closed position, the fluid pressure can be increased in front of the window to above hydrostatic pressure by the pump. Subsequent of opening the exit port creates a sudden pressure difference that flushes the flowline fluid, e.g. to the borehole. The sudden movement of dense fluid in front of the window dislodges and carries away window contamination. A 1000 psi (6.9 MPa) pressure pulse is generally sufficient in most cases.

All references referred to above are hereby incorporated by reference.

The foregoing outlines features of several embodiments so that those skilled in the art may better understand the aspects of the present disclosure. Those skilled in the art should appreciate that they may readily use the present disclosure as a basis for designing or modifying other processes and structures for carrying out the same purposes and/or achieving the same advantages of the embodiments introduced herein. Those skilled in the art should also realize that such equivalent constructions do not depart from the scope of the present disclosure, and that they may make various changes, substitutions and alterations herein without departing from such scope. 

The invention claimed is:
 1. A sensor for monitoring a hydrate inhibitor dissolved in a liquid, the sensor comprising: an internal reflection window configured to contact the liquid in use; a mid-infrared light source configured to direct a beam of mid-infrared radiation into the internal reflection window to provide for attenuated internal reflection at an interface between the internal reflection window and the liquid; a first narrow bandpass filter configured to preferentially transmit mid-infrared radiation over a band of wavelengths corresponding to an absorbance peak of the dissolved hydrate inhibitor to provide for filtering internally reflected mid-infrared radiation received from the internal reflection window; an infrared detector configured to detect the filtered mid-infrared radiation transmitted through the first filter, wherein the first narrow bandpass filter is located in between the internal reflection window and the infrared detector; and a processor arrangement, operably coupled to the infrared detector and configured to measure intensity of the detected mid-infrared radiation transmitted through the first narrow bandpass filter and determine an amount of the hydrate inhibitor dissolved in the liquid from the measured intensity.
 2. The sensor according to claim 1, wherein the first narrow bandpass filter is configured to preferentially transmit mid-infrared radiation over at least one of a band of wavelengths corresponding to: a 1040 cm⁻¹ absorbance peak for monoethylene glycol; a 1084 cm⁻¹ absorbance peak for monoethylene glycol; a 1020 cm⁻¹ absorbance peak for methanol; a 1045 cm⁻¹ absorbance peak for ethanol; and a 1295 cm⁻¹ absorbance peak for polyvinylpyrrolidone.
 3. The sensor according to claim 1, further comprising: a second narrow bandpass filter in between the internal reflection window and the infrared detector, the second narrow bandpass filter being configured to transmit mid-infrared radiation over a band of wavelengths corresponding to a reference portion of the absorbance spectrum of the liquid.
 4. The sensor according to claim 3, further comprising: the or a further infrared detector configured to detect filtered mid-infrared radiation transmitted through the second filter, wherein the processor arrangement is configured to measure a reference intensity of the detected mid-infrared radiation transmitted through the second filter and use the measured reference intensity in the determination of the amount of the hydrate inhibitor in the liquid.
 5. The sensor according to claim 1, wherein the first narrow bandpass filter comprises a plurality of the first narrow bandpass filters each configured to transmit mid-infrared radiation over a band of wavelengths corresponding to an absorbance peak of a respective hydrate inhibitor, and wherein the or a respective further infrared detector is configured to detect the filtered mid-infrared radiation transmitted through each of the plurality of the first narrow bandpass filters and the processor arrangement is configured to measure intensity of the detected mid-infrared radiation transmitted through each first narrow bandpass filter and determine therefrom an amount of each hydrate inhibitor in the liquid.
 6. The sensor according to claim 4, wherein the determined amounts of the hydrate inhibitor in the liquid is in the form of a ratio of the concentrations of the hydrate inhibitors.
 7. The sensor according to claim 1, wherein the beam of mid-infrared light is pulsed.
 8. The sensor according to claim 1, wherein the internal reflection window comprises one of a diamond window or a sapphire window.
 9. The sensor according to claim 1, further comprising: a heater configured to heat the internal reflection window.
 10. The sensor according to claim 1, further including: a pressure pulse arrangement configured to produce a pressure pulse in the fluid at the internal reflection window to clean a surface of the internal reflection window in contact with the fluid.
 11. The sensor according to claim 1, wherein the sensor is located subsea.
 12. A method of monitoring a hydrate inhibitor dissolved in a liquid, the method including: providing the sensor of claim 1 such that the internal reflection window is in direct contact with the liquid; and operating the sensor to determine an amount of the hydrate inhibitor dissolved in the liquid.
 13. A well or pipeline tool including the sensor of claim
 1. 14. A method for monitoring a hydrate inhibitor dissolved in a liquid, comprising: directing a beam of mid-infrared radiation into an internal reflection window that is in contact with the liquid; passing an attenuated internal reflection of the beam from an interface between the internal reflection window and the liquid through a narrow bandpass filter configured to preferentially transmit mid-infrared radiation over a band of wavelengths corresponding to an absorbance peak of the dissolved hydrate inhibitor; detecting the filtered mid-infrared radiation transmitted through the first filter; measuring an intensity of the detected mid-infrared radiation transmitted through the first filter; and determining an amount of the hydrate inhibitor dissolved in the liquid from the measured intensity.
 15. The method according to claim 14, wherein the narrow bandpass filter is configured to preferentially transmit mid-infrared radiation over at least one of a band of wavelengths corresponding to: a 1040 cm⁻¹ absorbance peak for monoethylene glycol; a 1084 cm⁻¹ absorbance peak for monoethylene glycol; a 1020 cm⁻¹ absorbance peak for methanol; a 1045 cm⁻¹ absorbance peak for ethanol; and a 1295 cm⁻¹ absorbance peak for polyvinylpyrrolidone.
 16. The method according to claim 14, further comprising: passing the attenuated internal reflection of the beam from the interface between the internal reflection window and the liquid through a reference narrow bandpass filter configured to transmit mid-infrared radiation over a band of wavelengths corresponding to a reference portion of the absorbance spectrum of the liquid.
 17. The method according to claim 16, further comprising: detecting a portion of the attenuated internal reflection of the beam from the interface between the internal reflection window and the liquid transmitted through the reference filter; measuring a reference intensity of the portion of the attenuated internal reflection of the beam from the interface between the internal reflection window and the liquid transmitted through the reference filter; and using the measured reference intensity in the determination of the amount of the hydrate inhibitor in the liquid. 